TY - JOUR
T1 - Detection of Hepatocellular Carcinoma and Liver Metastases with BR14
T2 - A Multicenter Phase IIA Study
AU - Hohmann, Joachim
AU - Müller, Anja
AU - Skrok, Jan
AU - Wolf, Karl Jürgen
AU - Martegani, Alberto
AU - Dietrich, Christoph F.
AU - Albrecht, Thomas
PY - 2012/3
Y1 - 2012/3
N2 - The study was designed primarily to find the optimal dosage range of BR14 contrast-enhanced ultrasonography (CEUS) to detect malignant focal liver lesions. Secondary objectives were the evaluation of the safety profile and comparison with contrast-enhanced MRI (CE MRI). We studied 25 patients (9 females, 16 males, mean age, 66 years) with known hepatocellular carcinoma or liver metastases at 3 centers over a 3-month period. Each patient underwent a baseline examination and at least 3 CEUS examinations with ascending dose levels (0.25 mL; 1.0 mL; 4.0 mL) of BR14. CE MRI was performed 4 weeks before or after the CEUS examination. Dedicated liver maps were used to record the location, size, and type of detected lesions. Examination quality was documented and safety parameters were assessed. The number of lesions detected by BR14 CEUS increased with dosage, whereas the number of missed lesions and the lesion sizes decreased. Despite the increasing contrast enhancement, substantial differences among dosages were not seen for other image quality parameters. No significant changes were noted in safety parameters and no serious adverse events were reported. We conclude that the recommended dose level of BR14 is between 1 mL and 4 mL; at this dosage, lesion detection is comparable to that of CE MRI.
AB - The study was designed primarily to find the optimal dosage range of BR14 contrast-enhanced ultrasonography (CEUS) to detect malignant focal liver lesions. Secondary objectives were the evaluation of the safety profile and comparison with contrast-enhanced MRI (CE MRI). We studied 25 patients (9 females, 16 males, mean age, 66 years) with known hepatocellular carcinoma or liver metastases at 3 centers over a 3-month period. Each patient underwent a baseline examination and at least 3 CEUS examinations with ascending dose levels (0.25 mL; 1.0 mL; 4.0 mL) of BR14. CE MRI was performed 4 weeks before or after the CEUS examination. Dedicated liver maps were used to record the location, size, and type of detected lesions. Examination quality was documented and safety parameters were assessed. The number of lesions detected by BR14 CEUS increased with dosage, whereas the number of missed lesions and the lesion sizes decreased. Despite the increasing contrast enhancement, substantial differences among dosages were not seen for other image quality parameters. No significant changes were noted in safety parameters and no serious adverse events were reported. We conclude that the recommended dose level of BR14 is between 1 mL and 4 mL; at this dosage, lesion detection is comparable to that of CE MRI.
KW - BR14
KW - Contrast agent
KW - Detection
KW - Hepatocellular carcinoma
KW - Liver metastases
KW - Phase IIa study
KW - Ultrasonography
UR - https://www.scopus.com/pages/publications/84856563206
UR - https://www.scopus.com/inward/citedby.url?scp=84856563206&partnerID=8YFLogxK
U2 - 10.1016/j.ultrasmedbio.2011.11.018
DO - 10.1016/j.ultrasmedbio.2011.11.018
M3 - Article
C2 - 22261514
AN - SCOPUS:84856563206
SN - 0301-5629
VL - 38
SP - 377
EP - 382
JO - Ultrasound in Medicine and Biology
JF - Ultrasound in Medicine and Biology
IS - 3
ER -